Case Study:  Patient: Sarah, a 20-year-old woman, presented with delayed puberty, lack of menstruation, and undeveloped breasts. Diagnosis: Kallmann syndrome (KS) confirmed by hormonal tests revealing low LH, FSH, and sex hormones. Investigation: Genetic testing identified a mutation in the KISS1 gene, known to affect GnRH function. However, GnRH deficiency persisted, suggesting another contributing factor. … Continue reading Exploring the GHRH Crossroads in Kallmann Syndrome